Senior Quality Engineer - Pharmaceutical or Medical Device at Gerresheimer

Peachtree City, Georgia, United States -

Full Time

Start Date

Immediate

Expiry Date

18 Dec, 25

Salary

0.0

Posted On

19 Sep, 25

Experience

5 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Validation, Quality Assurance, Regulatory Compliance, Documentation, Risk Management, GMP, ISO 13485, ISO 14971, ISO 15378, MDR, 21 CFR 820, Project Management, Statistical Methods, Problem-Solving, Interpersonal Skills, Communication Skills

Industry

Machinery Manufacturing

Description

Company Description Gerresheimer is an innovative systems and solutions provider for pharmaceutical primary packaging, drug delivery systems, medical devices and associated service, and as such a strategic partner for the global pharma and biotech industry. www.gerresheimer.com Job Description We’re looking for a detail-oriented and driven Validation Engineer to lead the planning, coordination, and execution of validation and qualification activities for both production and support processes. This role is essential to maintaining our high standards in compliance, documentation, and risk management in line with global regulatory requirements. Qualifications Independently plan and execute validation and qualification activities across projects Analyze test results, manage deviations, and evaluate changes impacting validated states Prepare and maintain comprehensive documentation in compliance with ISO and FDA standards Support internal and supplier audits, customer declarations, and requalification efforts Collaborate cross-functionally to support regulatory and quality compliance initiatives Contribute to continuous improvement in validation processes, documentation, and best practices Lead or support risk management activities during project execution Additional Information Required Qualifications Bachelor's degree in Mechanical Engineering, Industrial Engineering, or a related technical field Minimum of 5 years' experience in quality assurance, qualification, and/or validation Deep understanding of verification, validation, and regulatory standards Technical Expertise Solid knowledge of GMP, ISO 13485, ISO 14971, ISO 15378, MDR, and 21 CFR 820 Proficiency with digital systems including MES, ERP, Microsoft Office, Minitab, and quality management tools Advanced knowledge of statistical and problem-solving methods (e.g., Kepner-Tregoe) Skilled in project management principles and writing technical reports Personal Competencies Proactive, reliable, and flexible with a hands-on mindset Strong interpersonal skills and emotional resilience Excellent communication skills and ability to work well in cross-functional teams Fluent in English (German is a plus)

Responsibilities

Lead the planning, coordination, and execution of validation and qualification activities for production and support processes. Ensure compliance with global regulatory requirements and maintain high standards in documentation and risk management.